United Kingdom MHRA device registration 180308

Faecal specimen collection kit IVD, clinical

United Kingdom·In Vitro Diagnostic Device·Wuhan Ammunition Life-tech Co.,Ltd.·Registered Nov 19, 2024

Registration details

Device ID: 180308
MHRA Reference Number: 180308
Date Registered: Nov 19, 2024
Last Updated: Jul 31, 2024

Device classification

Device Type: In Vitro Diagnostic Device
Devices: Faecal specimen collection kit IVD, clinical
Type: IVD General

Manufacturer

Name: Wuhan Ammunition Life-tech Co.,Ltd.
Address: No. 04, 1st Floor, Building B10, Phase I, & No. 1 and No. 2, 2nd Floor, Building B21, Phase III, Block B, Wuhan Gaoke Medical Devices Park No. 818 Gaoxin Avenue, Wuhan East Lake High-Tech Development Zone, Wuhan City
Hubei Province, China
Created Date: Oct 16, 2023

Authorized Representative

Name: SUNGO Certification Company Limited
Relationship Type: UK Responsible Person
Address: 3rd Floor, 70 Gracechurch Street
London, England, United Kingdom
Postcode: EC3V 0HR

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About this record

Faecal specimen collection kit IVD, clinical is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 180308. The device is manufactured by Wuhan Ammunition Life-tech Co.,Ltd. from China, classified as In Vitro Diagnostic Device. The authorized representative in the UK is SUNGO Certification Company Limited.

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